具有D178N突变的遗传性朊病毒病中显著的PrPsc异质性。 - Suppr

Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation.

作者信息

Haïk Stéphane, Peoc'h Katell, Brandel Jean-Philippe, Privat Nicolas, Laplanche Jean-Louis, Faucheux Baptiste A, Hauw Jean-Jacques

出版信息

Ann Neurol. 2004 Dec;56(6):909-10; author reply 910-1. doi: 10.1002/ana.20327.

DOI:10.1002/ana.20327

PMID:15562434

Abstract

摘要

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Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation.

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Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation.

Ann Neurol. 2004 Dec;56(6):909-10; author reply 910-1. doi: 10.1002/ana.20327.

Prions and prion diseases.

Funct Neurol. 1999 Oct-Dec;14(4):241-52.

Human prion diseases: molecular and clinical aspects.

Arch Neurol. 2005 Apr;62(4):545-52. doi: 10.1001/archneur.62.4.545.

[The mystery of prion proteins: from neurodegenerative diseases to the biology of reproduction].

Ann Biol Clin (Paris). 2005 Mar-Apr;63(2):121-6.

[Prion diseases].

Bull Soc Sci Med Grand Duche Luxemb. 1994;131(2):41-3.

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PLoS Med. 2006 Feb;3(2):e14. doi: 10.1371/journal.pmed.0030014. Epub 2005 Dec 20.

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Amyloid. 2006 Jun;13(2):67-77. doi: 10.1080/13506120600722498.

In vitro self-propagation of recombinant PrPSc-like conformation generated in the yeast cytoplasm.

FEBS Lett. 2006 Jul 24;580(17):4231-5. doi: 10.1016/j.febslet.2006.06.074. Epub 2006 Jul 5.

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N Engl J Med. 1999 May 27;340(21):1675-7. doi: 10.1056/NEJM199905273402111.

Prion proteins: a biological role beyond prion diseases.

Acta Neurol Scand. 2007 Aug;116(2):75-82. doi: 10.1111/j.1600-0404.2007.00868.x.

引用本文的文献

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Neurol Genet. 2018 Aug 7;4(4):e253. doi: 10.1212/NXG.0000000000000253. eCollection 2018 Aug.

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Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation.

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